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Meenakshi Dabholkar, Frieda Bostick-Bruton, Christine Weber, Vilhelm A. Bohr, Charles Egwuagu, Eddie Reed, ERCC1 and ERCC2 Expression in Malignant Tissues From Ovarian Cancer Patients, JNCI: Journal of the National Cancer Institute, Volume 84, Issue 19, 7 October 1992, Pages 1512–1517, https://doi.org/10.1093/jnci/84.19.1512
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Abstract
Background: ERCC1 and ERCC2 are human DNA repair genes that are associated with in vitro resistance to selected DNA-damaging agents. Purpose: Fresh tumor tissues from 26 patients with ovarian cancer were analyzed for the RNA levels of expression of these genes to determine possible clinical relevance. Methods: Tumor tissues were harvested from patients immediately before they entered a cisplatin- or carboplatin-based treatment protocol. Clinical response was assessed by standard criteria. Gene expression level was assessed by slot blot analysis, using P-actin as a control. Relative expression levels were determined by comparing each tumor sample with a Chinese hamster ovary cell line that had a stable transfection of the human ERCC1 gene. Results: Patients who were clinically resistant to platinum-based therapy had a 2.6-fold higher expression level of ERCC1 in their tumor tissue than did patients who responded to that therapy ( P = .015). Results obtained by slot blot analysis were qualitatively confirmed by polymerase chain reaction analysis. Relative levels of expression of ERCC2 did not differ significantly between responders and non-responders. Conclusion: We conclude that ERCC1 expression levels in human tumor tissue may have a role in clinical resistance to platinum compounds. These data appear to be consistent with the assertion that ERCC1 serves as an excision nuclease, whereas ERCC2 serves as a helicase. [J Natl Cancer Inst 84:1512–1517, 1992]